FDA Label for Abatuss Dmx

View Indications, Usage & Precautions

Abatuss Dmx Product Label

The following document was submitted to the FDA by the labeler of this product Kramer Novis. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Active Ingredients(In Each 5 Ml Teaspoonful)



Dexchlorpheniramine maleate, USP 1 mg
Dextromethorphan HBr, USP 15 mg
Pseudoephedrine HCl, USP 30 mg


Purpose



Antihistamine
Cough suppressant
Nasal Decongestant


Uses



temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

  • sneezing
  • itchy nose or throat
  • runny nose
  • itchy, watery eyes
  • nasal congestion
  • temporarily controls cough due to minor throat and bronchial irritation associated with inhaled irritants
  • temporarily restores freer breathing through the nose

Warnings





Do Not Use If



you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.


Ask A Doctor Before Use If



you have

  • heart disease
  • high blood pressure
  • thyroid disease
  • diabetes
  • glaucoma
  • cough that occurs with too much phlegm (mucus)
  • trouble urinating due to an enlarged prostrate gland
  • a breathing problem or chronic cough that lasts or occurs with smoking, asthman, chronic bronchitis or emphysema

Ask A Doctor Or Pharmacist Before Use If You Are Taking Sedatives Or Tranquilizers





When Using This Product



  • do not exceed recommended dosage
  • excitability may occur especially in children
  • marked drowsiness may occur
  • alcohol, sedatives, and tranquilizers may increase the drowsiness effect
  • avoid alcoholic beverages while taking this product
  • do not take this product if you are taking sedatives or tranquilizers, without first consulting your doctor
  • use caution when driving a motor vehicle or operating machinery

Stop Use And Ask A Doctor If



  • nervousness, dizziness, or sleeplessness occur
  • new symtoms occur
  • symptoms do not improve within 7 days or are accompanied by fever
  • cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious conditions.

If Pregnant Or Breastfeeding



ask a health professional before use.


Keep Out Of Reach Of Children.



In case of accidental overdose, get medical help or contact a Poison Control Center right away.


Directions




  • do not take more than 4 doses in any 24-hour period
  • EVERY 6 HOURS
    Adults and children 12 years of age and older:
    10 mL (2 tsp)
    Children 6 to under 12 years of age:
    5 mL (1 tsp)
    Children 2 to under 6 years of age:
    consult a physician

Other Information



  • Store at room temperature 15°C-30°C (59°F-86°F)
  • protect from freezing
  • protect from light
  • Avoid excessive heat or humidity
  • TAMPER EVIDENT: Do not use this product if breakaway band on cap is broken on missing

Inactive Ingredients



Art. Flavor, Citric Acid, D&C Red #33, FD&C Blue #1, Glycerin, Sodium benzoate, Sodium saccharin, Sorbitol, Water


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